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Pretzel syndrome: Difference between revisions

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<ref>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720125/
<ref>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720125/
Rapamycin Prevents Seizures After Depletion of STRADA in a Rare Neurodevelopmental Disorder]</ref>
Rapamycin Prevents Seizures After Depletion of STRADA in a Rare Neurodevelopmental Disorder]</ref>
Due to the peculiar positioning of the legs due to the muscular hypotonia in combination with connective tissue problems, children with mutations in the STRADA/LYK5 gene can twist themselves into a pretzel-like configuration.<ref>[http://epilepsygenetics.net/2013/05/03/strada-mutations-mtor-activation-and-personalized-medicine-using-rapamycin/]</ref>
==Treatment==
==Treatment==
<ref>http://search.proquest.com/openview/c03b6627d94eb71e741206889933794f/1.pdf?pq-origsite=gscholar&cbl=33975</ref>
<ref>http://search.proquest.com/openview/c03b6627d94eb71e741206889933794f/1.pdf?pq-origsite=gscholar&cbl=33975</ref>

Revision as of 01:23, 4 May 2017

Pretzel syndrome or PMSE is a rare disorder characterized by skeletal deformity, malformation of the brain (with accompanying seizures), electrolyte imbalances, and variable malformations of the heart and other organs [1]

Due to the peculiar positioning of the legs due to the muscular hypotonia in combination with connective tissue problems, children with mutations in the STRADA/LYK5 gene can twist themselves into a pretzel-like configuration.[2]


Treatment

[3] [4]

Links

Polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome Q17143464 at Wikidata  Interwiki via Wikidata